4.7 Article

q-PCR-based assay for the toxic dinoflagellate Karenia selliformis monitoring along the Tunisian coasts

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 41, Pages 57486-57498

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-14597-9

Keywords

Toxic microalgae; Karenia selliformis; Tunisian costs; q-PCR; Hydrolysis probe; ITS1-5; 8S-ITS2 region

Funding

  1. Key Program of the Tunisian Ministry of Higher Education and Scientific Research [PRF-2017-D1P2]

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A quantitative-PCR assay based on the ITS molecular marker was developed for detecting and quantifying K. selliformis, with high specificity and a low detection limit. This assay shows potential for field application in monitoring K. selliformis blooms.
Karenia selliformis is a marine dinoflagellate responsible for fish-kill events. Its presence has been reported along the Tunisian coasts (south-eastern Mediterranean Sea) since the 1990s. In the present study, a quantitative-PCR assay, based on the internal transcribed spacer (ITS) molecular marker, was developed to detect and quantify K. selliformis in environmental bivalve mollusk samples and in seawater samples. The assay was optimized, and its specificity was confirmed using cross-reactivity experiments against microalgal species commonly found on the Tunisian coasts and/or closely related to K. selliformis. Calibration curves were performed by tenfold dilutions of plasmid DNA harboring target sequence and genomic DNA, attaining a limit of detection of around 5 copies of target DNA per reaction, far below one K. selliformis cell per reaction. The field application of the developed assay showed a powerful detection capability. Thus, the designed assay could contribute to the deployment of in-field diagnostic tools for K. selliformis blooms monitoring.

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